| NDC Code | 50844-392-15 |
|---|
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (50844-392-15) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
|---|
| Product NDC | 50844-392 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Ibuprofen |
|---|
| Non-Proprietary Name | Ibuprofen |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 19990301 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA075139 |
|---|
| Manufacturer | L.N.K. International, Inc. |
|---|
| Substance Name | IBUPROFEN |
|---|
| Strength | 200 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC] |
|---|